Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology, 2-24-16 Naka-Cho, Koganei, Tokyo 184-8588, Japan.
School of Biotechnology & Bioscience, Tokyo University of Technology, 1404-1 Katakura-Machi, Hachioji, Tokyo 192-0982, Japan.
Biosens Bioelectron. 2017 Jul 15;93:118-123. doi: 10.1016/j.bios.2016.09.060. Epub 2016 Sep 17.
DNA methylation level at a certain gene region is considered as a new type of biomarker for diagnosis and its miniaturized and rapid detection system is required for diagnosis. Here we have developed a simple electrochemical detection system for DNA methylation using methyl CpG-binding domain (MBD) and a glucose dehydrogenase (GDH)-fused zinc finger protein. This analytical system consists of three steps: (1) methylated DNA collection by MBD, (2) PCR amplification of a target genomic region among collected methylated DNA, and (3) electrochemical detection of the PCR products using a GDH-fused zinc finger protein. With this system, we have successfully measured the methylation levels at the promoter region of the androgen receptor gene in 10 copies of genomic DNA extracted from PC3 and TSU-PR1 cancer cell lines. Since no sequence analysis or enzymatic digestion is required for this detection system, DNA methylation levels can be measured within 3h with a simple procedure.
特定基因区域的 DNA 甲基化水平被认为是一种新的诊断生物标志物,因此需要一种小型化、快速的检测系统来进行诊断。在这里,我们开发了一种使用甲基化 CpG 结合域 (MBD) 和融合了葡萄糖脱氢酶 (GDH) 的锌指蛋白的简单电化学检测系统来检测 DNA 甲基化。该分析系统包括三个步骤:(1) 通过 MBD 收集甲基化 DNA,(2) 收集的甲基化 DNA 中目标基因组区域的 PCR 扩增,以及 (3) 使用融合了 GDH 的锌指蛋白对 PCR 产物进行电化学检测。使用该系统,我们成功地测量了从 PC3 和 TSU-PR1 癌细胞系提取的 10 个基因组 DNA 拷贝中雄激素受体基因启动子区域的甲基化水平。由于该检测系统不需要序列分析或酶切,因此可以在 3 小时内通过简单的步骤测量 DNA 甲基化水平。